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用于甲型流感病毒诱导包装的合成细胞系

Synthetic Cell Lines for Inducible Packaging of Influenza A Virus.

作者信息

Phan Thu, Ye Qian, Stach Christopher, Lin Yu-Chieh, Cao Haoyu, Bowen Annika, Langlois Ryan A, Hu Wei-Shou

机构信息

Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, Minnesota 55455, United States.

State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, P. R. China.

出版信息

ACS Synth Biol. 2024 Feb 16;13(2):546-557. doi: 10.1021/acssynbio.3c00526. Epub 2024 Jan 23.

Abstract

Influenza A virus (IAV) is a negative-sense RNA virus that causes seasonal infections and periodic pandemics, inflicting huge economic and human costs on society. The current production of influenza virus for vaccines is initiated by generating a seed virus through the transfection of multiple plasmids in HEK293 cells followed by the infection of seed viruses into embryonated chicken eggs or cultured mammalian cells. We took a system design and synthetic biology approach to engineer cell lines that can be induced to produce all viral components except hemagglutinin (HA) and neuraminidase (NA), which are the antigens that specify the variants of IAV. Upon the transfection of HA and NA, the cell line can produce infectious IAV particles. RNA-Seq transcriptome analysis revealed inefficient synthesis of viral RNA and upregulated expression of genes involved in host response to viral infection as potential limiting factors and offered possible targets for enhancing the productivity of the synthetic cell line. Overall, we showed for the first time that it was possible to create packaging cell lines for the production of a cytopathic negative-sense RNA virus. The approach allows for the exploitation of altered kinetics of the synthesis of viral components and offers a new method for manufacturing viral vaccines.

摘要

甲型流感病毒(IAV)是一种负链RNA病毒,可引起季节性感染和周期性大流行,给社会造成巨大的经济和人力成本。目前用于疫苗生产的流感病毒是通过在HEK293细胞中转染多个质粒产生种子病毒,然后将种子病毒感染入鸡胚或培养的哺乳动物细胞来启动生产的。我们采用系统设计和合成生物学方法构建细胞系,该细胞系可被诱导产生除血凝素(HA)和神经氨酸酶(NA)之外的所有病毒成分,HA和NA是确定IAV变体的抗原。转染HA和NA后,该细胞系可产生具有感染性的IAV颗粒。RNA测序转录组分析显示,病毒RNA合成效率低下以及宿主对病毒感染反应相关基因的表达上调是潜在的限制因素,并为提高合成细胞系的生产力提供了可能的靶点。总体而言,我们首次证明了有可能创建用于生产细胞病变性负链RNA病毒的包装细胞系。该方法允许利用病毒成分合成动力学的改变,并为制造病毒疫苗提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6ce/10878389/cb9920045ead/sb3c00526_0001.jpg

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